Vicente Bravo, S.L.
FDA import alert and refusal historySan Gines, SpainFEI 3004260599
As of October 26, 2026, Vicente Bravo, S.L. (San Gines, Spain) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for lemon peel, published by FDA on August 22, 2011, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Vicente Bravo, S.L.
3 records, newest first. Each line links to the FDA page it came from.
2018
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2012
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2011
- Import alert listingListed on Import Alert 99-08red listLemon PeelSource
Questions about Vicente Bravo, S.L.
- Is Vicente Bravo, S.L. on an FDA import alert?
- Yes. As of October 26, 2026, Vicente Bravo, S.L. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for lemon peel; FDA published the listing on August 22, 2011.
- Has FDA refused shipments from Vicente Bravo, S.L.?
- No FDA import refusals for Vicente Bravo, S.L. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Vicente Bravo, S.L. last inspected by FDA?
- FDA's most recent inspection of Vicente Bravo, S.L. with a final classification is dated September 6, 2018 and was classified NAI (No Action Indicated).
- What is Vicente Bravo, S.L.'s FEI number?
- Vicente Bravo, S.L.'s FDA Establishment Identifier (FEI) is 3004260599.
- Can shipments from Vicente Bravo, S.L. still enter the U.S.?
- Shipments of lemon peel from Vicente Bravo, S.L. can be detained without physical examination under Import Alert 99-08; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.